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DO Term : osteogenesis imperfecta type 8 [DOID:0110336] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An osteogenesis imperfecta that has_material_basis_in mutation in the P3H1 gene on chromosome 1p34.2.

synonyms:
ICD10CM:Q78.0,
OMIM:610915,
OI8,
osteogenesis imperfecta type VIII,
GARD:10152,
610915

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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